M05081
by Intensiv Medical Products IMPROMEDIFORM GmbH
Ref M05081Model M03075
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Overview
The M05081 medical device is a Class IIa implantable product, available for sterilization with the IMF approval. It is designed to be used in intensive care settings and has undergone professional testing. The device meets regulatory standards and is manufactured by Intensiv Medical Products IMPROMEDIFORM GmbH.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number4049051A03020101EXXXGXXMM 04049051014259 | Date20 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- M03075, M05081
- Primary DI / UDI-DI
- 04049051014259
- Basic UDI-DI
- 4049051A03020101EXXXGXXMM
- EMDN Code
- A03020101 Low pressure extension lines
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000014610
Other devices from Intensiv Medical Products IMPROMEDIFORM GmbH
See all devices from Intensiv Medical Products IMPROMEDIFORM GmbH →
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No